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16¼¼ ÀÌ»ó 1ȸ 1Á¤(10mg), 1ÀÏ 2Á¤(20mg)±îÁö º¹¿ëÇÒ ¼ö ÀÖ´Ù.
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| Related FDA Approved Drug |
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| Mechanism of Action |
Famotidine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Famotidine binds competitively to H2-receptors located on the basolateral membrane of the parietal cell, blocking histamine affects. This competitive inhibition results in reduced basal and nocturnal gastric acid secretion and a reduction in gastric volume, acidity, and amount of gastric acid released in response to stimuli including food, caffeine, insulin, betazole, or pentagastrin.
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| Pharmacology |
Famotidine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Famotidine, a competitive histamine H2-receptor antagonist, is used to treat gastrointestinal disorders such as gastric or duodenal ulcer, gastroesophageal reflux disease, and pathological hypersecretory conditions. Famotidine inhibits many of the isoenzymes of the hepatic CYP450 enzyme system. Other actions of Famotidine include an increase in gastric bacterial flora such as nitrate-reducing organisms.
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| Metabolism |
Famotidine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2C19 (CYP2C19)
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| Protein Binding |
Famotidine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 15-20%
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| Half-life |
Famotidine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2.5-3.5 hours
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| Absorption |
Famotidine¿¡ ´ëÇÑ Absorption Á¤º¸ The bioavailability of oral doses is 40-45%.
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| Pharmacokinetics |
FamotidineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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- ÀÛ¿ëÁö¼Ó½Ã°£ : 10-12 ½Ã°£
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| Biotransformation |
Famotidine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic.
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| Toxicity |
Famotidine¿¡ ´ëÇÑ Toxicity Á¤º¸ Intravenous, mouse: LD50 = 244.4mg/kg; Oral, mouse: LD50 = 4686 mg/kg. Symptoms of overdose include emesis, restlessness, pallor of mucous membranes or redness of mouth and ears, hypotension, tachycardia and collapse.
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| Drug Interactions |
Famotidine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Atazanavir This gastric pH modifier decreases the levels/effects of atazanavirEnoxacin The agent decreases the absorption of enoxacinItraconazole The anti-H2 decreases the absorption of the imidazoleKetoconazole The anti-H2 decreases the absorption of the imidazole
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Famotidine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals, food may slightly increase the product's bioavailability.Limit caffeine intake.Avoid alcohol.
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| Drug Target |
[Drug Target]
|
| Description |
Famotidine¿¡ ´ëÇÑ Description Á¤º¸ A competitive histamine H2-receptor antagonist. Its main pharmacodynamic effect is the inhibition of gastric secretion. [PubChem]
|
| Dosage Form |
Famotidine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Solution IntravenousTablet Oral
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| Drug Category |
Famotidine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Ulcer AgentsHistamine H2 Antagonists
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| Smiles String Canonical |
Famotidine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC(N)=NC1=NC(CSCCC(N)=NS(N)(=O)=O)=CS1
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| Smiles String Isomeric |
Famotidine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ N\C(N)=N\C1=NC(CSCC\C(N)=N\S(N)(=O)=O)=CS1
|
| InChI Identifier |
Famotidine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C8H15N7O2S3/c9-6(15-20(12,16)17)1-2-18-3-5-4-19-8(13-5)14-7(10)11/h4H,1-3H2,(H2,9,15)(H2,12,16,17)(H4,10,11,13,14)/f/h9-12H2
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| Chemical IUPAC Name |
Famotidine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 3-[[2-(diaminomethylideneamino)-1,3-thiazol-4-yl]methylsulfanyl]-N'-sulfamoylpropanimidamide
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| Drug-Induced Toxicity Related Proteins |
FAMOTIDINE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Granulocyte colony-stimulating factor receptor Drug:famotidine Toxicity:less reduced growth. drug-induced bone marrow failure. [¹Ù·Î°¡±â] Replated Protein:Granulocyte-macrophage colony-stimulating factor Drug:famotidine Toxicity:less reduced growth. drug-induced bone marrow failure. [¹Ù·Î°¡±â] Replated Protein:Interleukin-3 Drug:famotidine Toxicity:less reduced growth. drug-induced bone marrow failure. [¹Ù·Î°¡±â]
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